US9247764B2 - Nutritional composition containing oligosaccharide mixture - Google Patents
Nutritional composition containing oligosaccharide mixture Download PDFInfo
- Publication number
- US9247764B2 US9247764B2 US14/499,546 US201414499546A US9247764B2 US 9247764 B2 US9247764 B2 US 9247764B2 US 201414499546 A US201414499546 A US 201414499546A US 9247764 B2 US9247764 B2 US 9247764B2
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- US
- United States
- Prior art keywords
- oligosaccharide
- galβ1
- 4glc
- oligosaccharides
- mixture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 150000003271 galactooligosaccharides Chemical class 0.000 claims abstract description 24
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- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2002/00—Food compositions, function of food ingredients or processes for food or foodstuffs
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- A—HUMAN NECESSITIES
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- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
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- A23V2200/30—Foods, ingredients or supplements having a functional effect on health
- A23V2200/332—Promoters of weight control and weight loss
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
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- A23V2250/156—Mineral combination
-
- A—HUMAN NECESSITIES
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- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
- A23V2250/00—Food ingredients
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23V—INDEXING SCHEME RELATING TO FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES AND LACTIC OR PROPIONIC ACID BACTERIA USED IN FOODSTUFFS OR FOOD PREPARATION
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- A23V2250/70—Vitamins
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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- A23V2250/00—Food ingredients
- A23V2250/70—Vitamins
- A23V2250/704—Vitamin B
Definitions
- the invention relates to a nutritional composition such as an infant formula supplemented with an oligosaccharide mixture.
- the human colon is colonised with a wide range of bacteria that have both positive and negative effects on gut physiology as well as having other systemic influences.
- Predominant groups of bacteria found in the colon include bacteroides , bifidobacteria, eubacteria, clostridia and lactobacilli.
- the bacteria present have fluctuating activities in response to substrate availability, redox potential, pH, 0 2 tension and distribution in the colon.
- intestinal bacteria can be divided into species that exert either potentially harmful or beneficial effects on the host.
- Pathogenic effects (which may be caused by clostridia or bacteroides , for example) include diarrhoea, infections, liver damage, carcinogenesis and intestinal putrefaction.
- Health-promoting effects may be caused by the inhibition of growth of harmful bacteria, stimulation of immune functions, improving digestion and absorption of essential nutrients and synthesis of vitamins.
- An increase in numbers and/or activities of bacterial groups (such as Bifidobacterium and Lactobacillus ) that may have health promoting properties is desirable.
- the gastro-intestinal tract of a baby is thought to be sterile. During the process of birth, it encounters bacteria from the digestive tract and skin of the mother and starts to become colonised. Large differences exist with respect to the composition of the gut microbiota in response to the infant's feeding.
- the faecal flora of breast-fed infants includes appreciable populations of Bifidobacteria with some Lactobacillus species, whereas formula-fed infants have more complex microbiota, with Bifidobacteria, Bacteroides , Clostridia and Streptococci all usually present. After weaning, a pattern of gut microbiota that resembles the adult pattern becomes established.
- a prebiotic is a non-digestible food ingredient that beneficially affects the host by selectively stimulating the growth and/or activity of one or a limited number of bacteria in the colon, and thus improves host health.
- Such ingredients are non-digestible in the sense that they are not broken down and absorbed in the stomach or small intestine and thus pass intact to the colon where they are selectively fermented by the beneficial bacteria.
- prebiotics include certain oligosaccharides, such as fructooligosaccharides (FOS) and galactooligosaccharides (GOS).
- Human milk is known to contain a larger amount of indigestible oligosaccharides than most other animal milks.
- indigestible oligosaccharides represent the third largest solid component (after lactose and lipids) in breast milk, occurring at a concentration of 12-15 g/l in colostrum and 5-8 g/l in mature milk.
- Human milk oligosaccharides are very resistant to enzymatic hydrolysis, indicating that these oligosaccharides may display essential functions not directly related to their calorific value.
- US Patent Application No. 2003/0129278 describes an oligosaccharide mixture based on oligosaccharides produced from one or several animal milks which is characterized in that it comprises at least two oligosaccharide fractions which are each composed of at least two different oligosaccharides, with free lactose not pertaining thereto.
- the total spectrum of the oligosaccharides present in the oligosaccharide mixture differs from those present in the animal milk or animal milks from which the oligosaccharide fractions were extracted.
- oligosaccharides are extracted from only one animal milk, the proportion of neutral oligosaccharides to acidic (sialylated) oligosaccharides is 90-60:10-40 weight %, or b) if said oligosaccharides are extracted from at least two animal milks, the oligosaccharides extracted from two different animal milks each make up 10 weight % of the total amount of oligosaccharides present in the oligosaccharide mixture.
- WO2007/090894 describes an oligosaccharide mixture which comprises 5 to 70 wt % of at least one N-acetylated oligosaccharide, 20 to 90 wt % of at least one neutral galacto-oligosaccharide and 5 to 50 wt % of at least one sialylated oligosaccharide.
- oligosaccharide prebiotics Most research interest has focused on the fermentability and bifidogenicity of oligosaccharide prebiotics.
- in vitro studies have shown that a number of oligosaccharide prebiotics mimic the eukaryotic cell surface receptors to which virulent bacteria adhere as part of the pathogenicity process (Shoaf et al, 2006).
- trans-galacto-oligosaccharides have been found to enhance the protective abilities of Bifidobacterium breve in mice infected with Salmonella enterica (Asahara et al, 2001).
- Other potential benefits of prebiotics have also been investigated in adults including immunomodulatory properties, bone mineralisation and cardiovascular effects.
- US Patent Application No. 2003/0129278 describes an oligosaccharide mixture based on oligosaccharides produced from one or several animal milks which is characterized in that it comprises at least two oligosaccharide fractions which are each composed of at least two different oligosaccharides, with free lactose not pertaining thereto.
- the total spectrum of the oligosaccharides present in the oligosaccharide mixture differs from those present in the animal milk or animal milks from which the oligosaccharide fractions were extracted.
- oligosaccharides are extracted from only one animal milk, the proportion of neutral oligosaccharides to acidic (sialylated) oligosaccharides is 90-60:10-40 weight %, or b) if said oligosaccharides are extracted from at least two animal milks, the oligosaccharides extracted from two different animal milks each make up 10 weight % of the total amount of oligosaccharides present in the oligosaccharide mixture.
- WO2007/090894 describes an oligosaccharide mixture which comprises 5 to 70 wt % of at least one N-acetylated oligosaccharide, 20 to 90 wt % of at least one neutral galacto-oligosaccharide and 5 to 50 wt % of at least one sialylated oligosaccharide.
- the present inventors have surprisingly discovered that the administration of a mixture of prebiotic oligosaccharides comprising galacto-oligosaccharides with small quantities of more complex oligosaccharide species such as sialylated oligosaccharides and non-sialylated oligosaccharides including at least one N-acetyl group to germ-free mice inoculated with a human baby microbiota modulates lipid metabolism by reducing lipogenesis and promoting fatty acid beta-oxidation as compared with a control group not receiving the oligosaccharide mixture.
- the present invention provides the use of an N-acetylated oligosaccharide, a galacto-oligosaccharide and a sialylated oligosaccharide in the manufacture of a nutritional composition for administration to an infant in the first six months of life to reduce the risk of obesity later in life.
- the invention extends to a nutritional composition for administration to an infant which composition comprises, on a dry matter basis, from 2.5 to 15.0 wt % of an oligosaccharide mixture consisting of N-acetylated oligosaccharide(s), galacto-oligosaccharide(s) and sialylated oligosaccharide(s) with the proviso that the composition comprises at least 0.02 wt % of an N-acetylated oligosaccharide, at least 2.0 wt % of a galacto-oligosaccharide and at least 0.04 wt % of a sialylated oligosaccharide and that the N-acetylated oligosaccharide(s) comprise 0.5 to 4.0% of the oligosaccharide mixture, the galacto-oligosaccharide(s) comprise 92.0 to 98.5% of the oligosaccharide mixture and the sialylated oligo
- the benefits of a nutritional composition according to the invention extend to reduction of lipogenesis and higher beta-oxidation of fatty acids.
- the oligosaccharide mixture may be derived from animal milk, such as one or more of cows' milk, goats' milk or buffalo milk.
- the nutritional composition is an infant formula, but it may be any food or drink consumed by infants in the first few months of life including a therapeutic nutritional composition meeting the requirements of the EU regulations governing Foods for Special Medical Purposes (FSMP).
- FSMP Special Medical Purposes
- MTTP microsomal triglyceride transfer protein
- FOS fatty acid synthase
- galacto-oligosaccharide means an oligosaccharide comprising two or more galactose molecules which has no charge and no N-acetyl residue;
- infant means a child under the age of 12 months
- infant formula means a foodstuff intended for the complete nutrition of infants during the first four to six months of life. (Article 1.2 of the European Commission Directive 91/321/EEC of 14 May 1991 on infant formulae and follow-on formulae);
- N-acetylated oligosaccharide means an oligosaccharide having an N-acetyl residue
- oligosaccharide means a carbohydrate having a degree of polymerisation (DP) ranging from 2 to 20 inclusive but not including lactose;
- prebiotic means a selectively fermented ingredient that allows specific changes, both in the composition and/or activity in the gastrointestinal microbiota that confers benefits upon host well-being and health (Bouhnik et al, 2004);
- sialylated oligosaccharide means an oligosaccharide having a sialic acid residue with associated charge.
- Suitable N-acetylated oligosaccharides include GalNAc ⁇ 1,3Gal ⁇ 1,4Glc and Gal ⁇ 1,6GalNAc ⁇ 1,3Gal ⁇ 1,4Glc.
- the N-acetylated oligosaccharides may be prepared by the action of glucosaminidase and/or galactosaminidase on N-acetyl-glucose and/or N-acetyl galactose. Equally, N-acetyl-galactosyl transferases and/or N-acetyl-glycosyl transferases may be used for this purpose.
- keto-hexoses e.g. fructose
- Suitable galacto-oligosaccharides include Gal ⁇ 1,6Gal, Gal ⁇ 1,6Gal ⁇ 1,4Glc Gal ⁇ 1,6Gal ⁇ 1,6Glc, Gal ⁇ 1,3Gal ⁇ 1,3Glc, Gal ⁇ 1,3Gal ⁇ 1,4Glc, Gal ⁇ 1,6Gal ⁇ 1,6Gal ⁇ 1,4Glc, Gal ⁇ 1,6Gal ⁇ 1,3Gal ⁇ I,4Glc, Gal ⁇ 1,3Gal ⁇ 1,6Gal ⁇ 1,4Glc, Gal ⁇ 1,3Gal ⁇ 1,3Gal ⁇ 1,4Glc, Gal ⁇ 1,4Gal ⁇ 1,4Glc and Gal ⁇ 1,4Gal ⁇ 1,4Gal ⁇ 1,4Glc.
- Gal ⁇ 1,6Gal ⁇ 1,4Glc Gal ⁇ 1,6Gal ⁇ 1,6Glc
- Gal ⁇ 1,3Gal ⁇ 1,4Glc Gal ⁇ 1,6Gal ⁇ 1,6Gal ⁇ 1,4Glc
- Gal ⁇ 1,6Gal ⁇ 1,3Gal ⁇ 1,4Glc Gal ⁇ 1,3Gal ⁇ 1,6Gal ⁇ 1,4Glc
- Gal ⁇ 1,4Gal ⁇ 1,4Glc and Gal ⁇ 1,4Gal ⁇ 1,4Gal ⁇ ,4Glc and mixtures thereof are commercially available under the trade marks Vivinal® and Elix'or®.
- oligosaccharides are Dextra Laboratories, Sigma-Aldrich Chemie GmbH and Kyowa Hakko Kogyo Co., Ltd.
- specific glycoslytransferases such as galactosyltransferases may be used to produce neutral oligosaccharides.
- DP polymerisation
- the nutritional composition comprises 3.0 to 12.0% of the oligosaccharide mixture, more preferably from 4.0 to 7.0% of the oligosaccharide mixture.
- the nutritional composition preferably comprises at least 0.03 wt % of an N-acetylated oligosaccharide, at least 3.0 wt % of a galacto-oligosaccharide and at least 0.08 wt % of a sialylated oligosaccharide, more preferably at least 0.04 wt % of an N-acetylated oligosaccharide, at least 4.0 wt % of a galacto-oligosaccharide and at least 0.09 wt % of a sialylated oligosaccharide.
- a nutritional composition according to the invention preferably also comprises at least one probiotic bacterial strain.
- a probiotic is a microbial cell preparation or components of microbial cells with a beneficial effect on the health or well-being of the host.
- Suitable probiotic bacterial strains include Lactobacillus rhamnosus ATCC 53103 obtainable from Valio Oy of Finland under the trade mark LGG, Lactobacillus rhamnosus CGMCC 1.3724 , Lactobacillus paracasei CNCM I-2116 , Lactobacillus reuteri ATCC 55730 and Lactobacillus reuteri DSM 17938 obtainable from Biogaia, Lactobacillus fermentum VRI 003, Streptococcus salivarius DSM 13084 sold by BLIS Technologies Limited of New Zealand under the designation K12 , Bifidobacterium lactis CNCM 1-3446 sold inter alia by the Christian Hansen company of Denmark under the trade mark Bb12 , Bifidobacterium longum
- the probiotic may be added in an amount between 10 3 and 10 12 cfu/g powder, more preferably between 10 7 and 10 12 cfu/g powder.
- the nutritional composition according to the invention is an infant formula.
- the general composition of an infant formula according to the invention will now be described by way of example.
- the formula contains a protein source.
- the type of protein is not believed to be critical to the present invention provided that the minimum requirements for essential amino acid content are met and satisfactory growth is ensured.
- protein sources based on whey, casein and mixtures thereof may be used as well as protein sources based on soy.
- the protein source may be based on acid whey or sweet whey or mixtures thereof and may include alpha-lactalbumin and beta-lactoglobulin in whatever proportions are desired.
- the proteins may be intact or hydrolysed or a mixture of intact and hydrolysed proteins. It may be desirable to supply partially hydrolysed proteins (degree of hydrolysis between 2 and 20%), for example for infants believed to be at risk of developing cows' milk allergy. If hydrolysed proteins are required, the hydrolysis process may be carried out as desired and as is known in the art. For example, a whey protein hydrolysate may be prepared by enzymatically hydrolysing the whey fraction in one or more steps. If the whey fraction used as the starting material is substantially lactose free, it is found that the protein suffers much less lysine blockage during the hydrolysis process. This enables the extent of lysine blockage to be reduced from about 15% by weight of total lysine to less than about 10% by weight of lysine; for example about 7% by weight of lysine which greatly improves the nutritional quality of the protein source.
- An infant formula according to the present invention contains a carbohydrate source.
- Any carbohydrate source conventionally found in infant formulae such as lactose, saccharose, maltodextrin, starch and mixtures thereof may be used although the preferred source of carbohydrates is lactose.
- the carbohydrate sources contribute between 35 and 65% of the total energy of the formula.
- An infant formula according to the present invention contains a source of lipids.
- the lipid source may be any lipid or fat which is suitable for use in infant formulas.
- Preferred fat sources include palm olein, high oleic sunflower oil and high oleic safflower oil.
- the essential fatty acids linoleic and ⁇ -linolenic acid may also be added as may small amounts of oils containing high quantities of preformed arachidonic acid and docosahexaenoic acid such as fish oils or microbial oils.
- the fat content is preferably such as to contribute between 30 to 55% of the total energy of the formula.
- the fat source preferably has a ratio of n-6 to n-3 fatty acids of about 5:1 to about 15:1; for example about 8:1 to about 10:1.
- the infant formula will also contain all vitamins and minerals understood to be essential in the daily diet and in nutritionally significant amounts. Minimum requirements have been established for certain vitamins and minerals, Examples of minerals, vitamins and other nutrients optionally present in the infant formula include vitamin A, vitamin 131, vitamin B2, vitamin B6, vitamin B 12, vitamin E, vitamin K, vitamin C, vitamin D, folic acid, inositol, niacin, biotin, pantothenic acid, choline, calcium, phosphorous, iodine, iron, magnesium, copper, zinc, manganese, chloride, potassium, sodium, selenium, chromium, molybdenum, taurine, and L-carnitine. Minerals are usually added in salt form. The presence and amounts of specific minerals and other vitamins will vary depending on the intended infant population.
- the infant formula may contain emulsifiers and stabilisers such as soy lecithin, citric acid esters of mono- and di-glycerides, and the like.
- the infant formula may optionally contain other substances which may have a beneficial effect such as lactoferrin, nucleotides, nucleosides, and the like.
- the formula will contain from 2.5 to 15.0 wt % of an oligosaccharide mixture consisting of N-acetylated oligosaccharide(s), galacto-oligosaccharide(s) and sialylated oligosaccharide(s) in amounts of at least 0.02 wt % of an N-acetylated oligosaccharide, at least 2.0 wt % of a galacto-oligosaccharide and at least 0.04 wt % of a sialylated oligosaccharide, the N-acetylated oligosaccharide(s) comprising 0.5 to 4.0% of the oligosaccharide mixture, the galacto-oligosaccharide(s) comprising 92.0 to 98.5% of the oligosaccharide mixture and the sialylated oligosaccharide(s) comprising 1.0 to 4.0% of the oligosaccharide mixture.
- the infant formula may be prepared by blending together the protein source, the carbohydrate source and the fat source in appropriate proportions.
- Emulsifiers may be added if desired. Vitamins and minerals may be added at this point but are usually added later to avoid thermal degradation. Any lipophilic vitamins, emulsifiers and the like may be dissolved into the fat source prior to blending. Water, preferably water which has been subjected to reverse osmosis, may then be mixed in to form a liquid mixture.
- the liquid mixture may then be thermally treated to reduce bacterial loads.
- the liquid mixture may be rapidly heated to a temperature in the range of about 80° C. to about 110° C. for about 5 seconds to about 5 minutes. This may be carried out by steam injection or by heat exchanger, e.g. a plate heat exchanger.
- the liquid mixture may then be cooled to about 60° C. to about 85° C., for example by flash cooling.
- the liquid mixture may then be homogenised, for example in two stages at about 7 MPa to about 40 MPa in the first stage and about 2 MPa to about 14 MPa in the second stage.
- the homogenised mixture may then be further cooled to add any heat sensitive components such as vitamins and minerals.
- the pH and solids content of the homogenised mixture is conveniently standardised at this point.
- the homogenised mixture is transferred to a suitable drying apparatus, such as a spray drier or freeze drier, and converted to powder.
- a suitable drying apparatus such as a spray drier or freeze drier
- the powder should have a moisture content of less than about 5% by weight.
- the oligosaccharides may be added directly to the infant formula by dry mixing.
- the infant formula according to the invention is fed to the baby at every feed.
- composition of an infant formula according to the present invention is given below.
- mice A total of 19 C3H female germ-free mice (Charles River, France) were housed under the same environmental conditions and were fed with a standard semi-synthetic irradiated rodent diet (Reeves et al, 1993). At 8 weeks of age, the germ-free mice received a single dose of human baby microbiota (HBM) bacteria mixture and were assigned randomly to 2 groups which followed different nutritional interventions over a 2 week period.
- HBM human baby microbiota
- Morning spot urines, blood plasma, and intact liver tissues were collected upon animal autopsy and snap-frozen prior to metabonomic analysis.
- Metabonomics using high resolution spectroscopic methods with subsequent multivariate statistical analyses is a well-established strategy for differential metabolic pathway profiling and assessment of dietary intervention effects and efficacy (Martin et al, 2008; Nicholson et al, 2005; Rezzi et al, 2007b; Rezzi et al, 2007; Stella et al, 2006).
- the metabolic profiles were mined with multivariate analytical methods to recover metabolic probes of oligosaccharide intervention, which serve as reference for describing and predicting groups of animals according to treatments (Table 1).
- Table 1 and FIG. 1 show that use of a nutritional composition according to the invention reduced triglyceride concentration in the liver.
- the control and experimental groups were compared using unpaired Student's t-test and the difference was statistical significant at 95% confidence level.
- Table 1 and FIG. 2 show that use of a nutritional composition according to the invention also reduced lipogenesis and triacylglycerol incorporation into lipoproteins in the liver, the measure Delta CT plotted on the y-axis in FIG. 2 being the difference between the threshold cycle of the gene of interest and that of the endogenous reference gene.
- the decrease in expression levels in animals in the experimental group was significant at 99.9% confidence level when using unpaired Student's t-test.
- mice in the control and experimental groups confirmed that mice in the experimental group had decreased hepatic triglycerides, lipogenic activities (FAS) and incorporation of triglycerides into lipoproteins (MTTP) ( FIG. 2 ).
- MTTP microsomal triglyceride transfer protein
- FOS fatty acid synthase
- the R x 2 value shows how much of the variation in the dataset X is explained by the model.
- the Q Y 2 value represents the predictability of the models, and relates to its statistical validity. Data are presented as area normalized intensities (a.u.) of representative metabolite signals as means ⁇ standard deviation (SD). The values for the HBM mice supplemented with prebiotics were compared to HBM control mice, *, and *** designate significant difference at 95% and 99.9% confidence level, respectively.
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Abstract
Description
Nutrient | per 100 kca1 | per litre | ||
Energy (kcal) | 100 | 670 | ||
Protein (g) | 1.83 | 12.3 | ||
Fat(g) | 5.3 | 35.7 | ||
Linoleic acid (g) | 0.79 | 5.3 | ||
A-Linolenic acid (mg) | 101 | 675 | ||
Lactose (g) | 11.2 | 74.7 | ||
Galacto-oli osaccharides (g) | 1.1 | 6.8 | ||
N-acetylated oligosaccharides (g) | 0.027 | 0.055 | ||
Sialylated oligosaccharides (g) | 0.027 | 0.134 | ||
Minerals (g) | 0.37 | 2.5 | ||
Na (mg) | 23 | 150 | ||
K (mg) | 89 | 590 | ||
Cl (mg) | 64 | 430 | ||
Ca (mg) | 62 | 410 | ||
P(mg) | 31 | 210 | ||
Mg (mg) | 7 | 50 | ||
Mn (μg) | 8 | 50 | ||
Se (μg) | 2 | 13 | ||
Vitamin A (μg RE) | 105 | 700 | ||
Vitamin D (μg) | 1.5 | 10 | ||
Vitamin E (mg TE) | 0.8 | 5.4 | ||
Vitamin K1 (μg) | 8 | 54 | ||
Vitamin C (mg) | 10 | 67 | ||
Vitamin B1 (mg) | 0.07 | 0.47 | ||
Vitamin B2 (mg) | 0.15 | 1.0 | ||
Niacin (mg) | 1 | 6.7 | ||
Vitamin B6 (mg) | 0.075 | 0.50 | ||
Folic acid (μg) | 9 | 60 | ||
Pantothenic acid (mg) | 0.45 | 3 | ||
Vitamin B12 (μg) | 0.3 | 2 | ||
Biotin (μg) | 2.2 | 15 | ||
Choline (mg) | 10 | 67 | ||
Fe (mg) | 1.2 | 8 | ||
I (μg) | 15 | 100 | ||
Cu (mg) | 0.06 | 0.4 | ||
Zn (mg) | 0.75 | 5 | ||
TABLE 1 |
Influential metabolites describing prebiotic metabolic effects |
in plasma, liver and urine |
Metabolite | Control Group | Experimental Group | ||
Plasma | Qy 2 = 29%, Rx 2 = 86% | |||
Lipoproteins | 0.5 ± 0.2 | 0.4 ± 0.1 | ||
Liver | QY 2 = 36%, Rx 2 = 46% | |||
Betaine | 1.6 ± 0.3 | 2.5 ± 0.2*** | ||
Choline | 0.5 ± 0.2 | 1.1 ± 0.2*** | ||
DMG | 0.06 ± 0.02 | 0.19 ± 0.05*** | ||
Tri 1 eerides | 3.6 ± 1.3 | 2.1 ± 0.4* | ||
Phosphocholine | 1.7 ± 0.3 | 2.4 ± 0.3*** | ||
Sarcosine | 0.14 ± 0.03 | 0.18 ± 0.02* | ||
Urine | QY 2 = 70%, Rx 2 = 49% | |||
Carnitine | 0.3 ± 0.06 | 5.2 ± 1.3*** | ||
N-acetyl-carnitine | 017 ± 0.02 | 1.3 ± 0.3*** | ||
α-keto-isocaroate | 1.3 ± 0.3 | 0.9 ± 0.1* | ||
α-aminoadiate | 0.33 ± 0.05 | 0.19 ± 0.02*** | ||
O-PLS models were generated with 1 predictive component, and 2 orthogonal components to discriminate between 2 groups of mice. The Rx 2 value shows how much of the variation in the dataset X is explained by the model. The QY 2 value represents the predictability of the models, and relates to its statistical validity. Data are presented as area normalized intensities (a.u.) of representative metabolite signals as means ± standard deviation (SD). The values for the HBM mice supplemented with prebiotics were compared to HBM control mice, *, and *** designate significant difference at 95% and 99.9% confidence level, respectively. |
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EP08159900A EP2143341A1 (en) | 2008-07-08 | 2008-07-08 | Nutritional Composition Containing Oligosaccharide Mixture |
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EPPCT/EP2009/047656 | 2009-06-19 | ||
US201113003467A | 2011-01-10 | 2011-01-10 | |
US13/860,229 US8846642B2 (en) | 2008-07-08 | 2013-04-10 | Nutritional composition containing oligosaccharide mixture |
US14/499,546 US9247764B2 (en) | 2008-07-08 | 2014-09-29 | Nutritional composition containing oligosaccharide mixture |
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US13/860,229 Division US8846642B2 (en) | 2008-07-08 | 2013-04-10 | Nutritional composition containing oligosaccharide mixture |
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US13/860,229 Active US8846642B2 (en) | 2008-07-08 | 2013-04-10 | Nutritional composition containing oligosaccharide mixture |
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US (3) | US8586563B2 (en) |
EP (2) | EP2143341A1 (en) |
CN (1) | CN102088871B (en) |
AU (1) | AU2009268222B2 (en) |
BR (1) | BRPI0915824A2 (en) |
CA (1) | CA2725039A1 (en) |
CL (1) | CL2009001560A1 (en) |
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MY (1) | MY155717A (en) |
RU (1) | RU2508743C2 (en) |
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TW (1) | TW201006392A (en) |
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- 2009-06-19 BR BRPI0915824-3A patent/BRPI0915824A2/en not_active Application Discontinuation
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Also Published As
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EP2309876B1 (en) | 2020-03-25 |
AU2009268222B2 (en) | 2015-06-25 |
CN102088871A (en) | 2011-06-08 |
US8846642B2 (en) | 2014-09-30 |
US20130224331A1 (en) | 2013-08-29 |
RU2011104195A (en) | 2012-08-20 |
US20150030720A1 (en) | 2015-01-29 |
BRPI0915824A2 (en) | 2015-08-04 |
MY155717A (en) | 2015-11-30 |
US8586563B2 (en) | 2013-11-19 |
MX2011000284A (en) | 2011-02-25 |
RU2508743C2 (en) | 2014-03-10 |
CA2725039A1 (en) | 2010-01-14 |
EP2143341A1 (en) | 2010-01-13 |
CL2009001560A1 (en) | 2011-04-29 |
EP2309876A1 (en) | 2011-04-20 |
WO2010003803A1 (en) | 2010-01-14 |
TW201006392A (en) | 2010-02-16 |
US20110110904A1 (en) | 2011-05-12 |
ES2785686T3 (en) | 2020-10-07 |
CN102088871B (en) | 2013-01-02 |
ZA201100971B (en) | 2012-07-25 |
SG192472A1 (en) | 2013-08-30 |
AU2009268222A1 (en) | 2010-01-14 |
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